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0003536898
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a) A. R. Bassindale and P. G. Taylor, 'The Chemistry of Organic Silicon Compounds,' Vol. 2, ed. by S. Patai and Z. Rappoport, John Wiley & Sons, Inc., New York, 1989, pp. 893-963;
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0030580396
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3)Li which could be prepared at -78 °C and was alkylated with alkyl iodides in good yields
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3)Li which could be prepared at -78 °C and was alkylated with alkyl iodides in good yields.
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Preliminary communication: M. Shimizu, T. Hata, and T. Hiyama, Tetrahedron Lett., 1997, 38, 4591.
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35
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0342829956
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Although 1,2-difluoro-1-silyloxiranes and 1,2,2-trifluoro-1-silyloxirane were reportedly prepared by epoxidation of the corresponding fluorosilylethenes (vide infra), the synthesis of 1-fluoro-1-silyloxiranes (5) has never been reported, to the best of our knowledge, a) T. Dubuffet, R. Sauvetre, and J.-F. Normant, J. Organomet. Chem., 1988, 354, 1;
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37
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0343322220
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note
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No product resulting from the Peterson elimination or the Brook rearrangement of 8 was observed.
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-
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38
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0001191318
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ed. by R. E. Banks, B. E. Smart, and J. C. Tatlow, Plenum Press, New York
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B.E. Smart, 'Organofluorine Chemistry-Principles and Commercial Applications,' ed. by R. E. Banks, B. E. Smart, and J. C. Tatlow, Plenum Press, New York, 1994, pp. 57-88.
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Smart, B.E.1
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39
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0001391988
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ed. by D. Barton and W. D. Ollis, Pergamon Press, Oxford
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a) I. Fleming, 'Comprehensive Organic Chemistry,' Vol. 3, ed. by D. Barton and W. D. Ollis, Pergamon Press, Oxford, 1979, pp. 541-686;
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Fleming, I.1
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40
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0343758214
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Ref. 5a; pp. 951-955
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b) Ref. 5a; pp. 951-955.
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-
-
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41
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0343322219
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note
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When i-propyl iodide or i-butyl iodide was used, protonated product (6) (R″ = H) formed which might have resulted from a proton abstraction from the iodide.
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